Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1017
Gene Symbol: CDK2
CDK2
CUI: C0026987
Disease: Myelofibrosis
Myelofibrosis 		0.010 GeneticVariation BEFREE These results suggested that mutation of the p16/CDKN2 gene was a common factor in the development of human MMMs and ACCs, while this gene may be correlated with development and/or progression of a subtype and play a role in the oncogenesis of these cancers. 17912431

2007